Therapeutic efficiency of Tamoxifen/Orlistat nanocrystals against solid ehrlich carcinoma via targeting TXNIP/HIF1-α/MMP-9/P27 and BAX/Bcl2/P53 signaling pathways

Orlistat (Orli) is an anti-obesity medication that has been approved by the US Food and Drug Administration. It has relatively limited oral bioavailability with promising inhibitory effects on cell proliferation as well as reducing the growth of tumors. This investigation was done to evaluate the po...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2024-11, Vol.180, p.117429, Article 117429
Hauptverfasser: El-Masry, Thanaa A., El-Nagar, Maysa M.F., Oriquat, Ghaleb Ali, Alotaibi, Badriyah S., Saad, Hebatallah M., El Zahaby, Enas I., Ibrahim, Hanaa A.
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container_start_page 117429
container_title Biomedicine & pharmacotherapy
container_volume 180
creator El-Masry, Thanaa A.
El-Nagar, Maysa M.F.
Oriquat, Ghaleb Ali
Alotaibi, Badriyah S.
Saad, Hebatallah M.
El Zahaby, Enas I.
Ibrahim, Hanaa A.
description Orlistat (Orli) is an anti-obesity medication that has been approved by the US Food and Drug Administration. It has relatively limited oral bioavailability with promising inhibitory effects on cell proliferation as well as reducing the growth of tumors. This investigation was done to evaluate the potential protective effect of Tamoxifen/Orlistat nanocrystals alone or in combination against Solid Ehrlich Carcinoma (SEC) and to clarify the possible underlying influences. The liquid antisolvent precipitation technique (bottom-up technology) was utilized to manufacture Orlistat Nanocrystals. To explore potential causes for the anti-tumor action, female Swiss Albino mice bearing SEC were randomly assigned into five equal groups (n = 6). Group 1: Tumor control group, group 2: Tam group: tamoxifen (0.01 g/kg, IP), group 3: Free-Orli group: orlistat (0.24 g/kg, IP), group 4: Nano-Orli: orlistat nanocrystals (0.24 g/kg, IP), group 5: Tam–Nano-Orli: Both doses of Tam and Nano-Orli. All treatments were administered for 16 days. The untreated mice showed development in the tumor volume and weight. As well as histopathology results from these mice revealed many tumor large cells as well as solid sheets of malignant cells. Also, untreated mice showed raised VEGF and TGF-1beta content. Moreover, results of gene expression in the SEC-bearing mice noted upregulation in HIF-1α, MMP-9, Bcl-2, and P27 gene expression and downregulation of TXNIP, BAX, and P53 gene expression. On the other hand, administrated TAM, Free-Orli, Nano-Orli, and a combination of Tam-Nano-Orli distinctly suppressed the tumor effects on estimated parameters with special reference to Tam-Nano-Orli. The developed Tamoxifen/Orlistat nanocrystals combination could be considered a promising approach to augment antitumor effects. [Display omitted] •Orlistat (Orli) is an anti-obesity medication.•Orli has limited oral bioavailability.•Orli has inhibitory effects on cell proliferation and reducing the growth of tumors.•Tamoxifen/Orlistat nanocrystals combination could have antitumor effects.
doi_str_mv 10.1016/j.biopha.2024.117429
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It has relatively limited oral bioavailability with promising inhibitory effects on cell proliferation as well as reducing the growth of tumors. This investigation was done to evaluate the potential protective effect of Tamoxifen/Orlistat nanocrystals alone or in combination against Solid Ehrlich Carcinoma (SEC) and to clarify the possible underlying influences. The liquid antisolvent precipitation technique (bottom-up technology) was utilized to manufacture Orlistat Nanocrystals. To explore potential causes for the anti-tumor action, female Swiss Albino mice bearing SEC were randomly assigned into five equal groups (n = 6). Group 1: Tumor control group, group 2: Tam group: tamoxifen (0.01 g/kg, IP), group 3: Free-Orli group: orlistat (0.24 g/kg, IP), group 4: Nano-Orli: orlistat nanocrystals (0.24 g/kg, IP), group 5: Tam–Nano-Orli: Both doses of Tam and Nano-Orli. All treatments were administered for 16 days. The untreated mice showed development in the tumor volume and weight. 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It has relatively limited oral bioavailability with promising inhibitory effects on cell proliferation as well as reducing the growth of tumors. This investigation was done to evaluate the potential protective effect of Tamoxifen/Orlistat nanocrystals alone or in combination against Solid Ehrlich Carcinoma (SEC) and to clarify the possible underlying influences. The liquid antisolvent precipitation technique (bottom-up technology) was utilized to manufacture Orlistat Nanocrystals. To explore potential causes for the anti-tumor action, female Swiss Albino mice bearing SEC were randomly assigned into five equal groups (n = 6). Group 1: Tumor control group, group 2: Tam group: tamoxifen (0.01 g/kg, IP), group 3: Free-Orli group: orlistat (0.24 g/kg, IP), group 4: Nano-Orli: orlistat nanocrystals (0.24 g/kg, IP), group 5: Tam–Nano-Orli: Both doses of Tam and Nano-Orli. All treatments were administered for 16 days. The untreated mice showed development in the tumor volume and weight. As well as histopathology results from these mice revealed many tumor large cells as well as solid sheets of malignant cells. Also, untreated mice showed raised VEGF and TGF-1beta content. Moreover, results of gene expression in the SEC-bearing mice noted upregulation in HIF-1α, MMP-9, Bcl-2, and P27 gene expression and downregulation of TXNIP, BAX, and P53 gene expression. On the other hand, administrated TAM, Free-Orli, Nano-Orli, and a combination of Tam-Nano-Orli distinctly suppressed the tumor effects on estimated parameters with special reference to Tam-Nano-Orli. The developed Tamoxifen/Orlistat nanocrystals combination could be considered a promising approach to augment antitumor effects. [Display omitted] •Orlistat (Orli) is an anti-obesity medication.•Orli has limited oral bioavailability.•Orli has inhibitory effects on cell proliferation and reducing the growth of tumors.•Tamoxifen/Orlistat nanocrystals combination could have antitumor effects.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>39293373</pmid><doi>10.1016/j.biopha.2024.117429</doi><oa>free_for_read</oa></addata></record>
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subjects Animals
Antitumar
bcl-2-Associated X Protein - genetics
bcl-2-Associated X Protein - metabolism
Carcinoma, Ehrlich Tumor - drug therapy
Carcinoma, Ehrlich Tumor - pathology
Carrier Proteins - metabolism
Female
Hypoxia-Inducible Factor 1, alpha Subunit - metabolism
Matrix Metalloproteinase 9 - genetics
Matrix Metalloproteinase 9 - metabolism
Mice
Nanocrystals
Nanoparticles - chemistry
Orlistat
Proto-Oncogene Proteins c-bcl-2 - genetics
Proto-Oncogene Proteins c-bcl-2 - metabolism
Signal Transduction - drug effects
Solid ehrlich carcinoma
Tamoxifen
Tamoxifen - pharmacology
Tumor Suppressor Protein p53 - genetics
Tumor Suppressor Protein p53 - metabolism
title Therapeutic efficiency of Tamoxifen/Orlistat nanocrystals against solid ehrlich carcinoma via targeting TXNIP/HIF1-α/MMP-9/P27 and BAX/Bcl2/P53 signaling pathways
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